@article{pittir20452,
          volume = {5},
          number = {10},
           month = {May},
          author = {W Du and DP Curran},
           title = {Synthesis of carbocyclic and heterocyclic fused quinolines by cascade radical annulations of unsaturated N-aryl thiocarbamates, thioamides, and thioureas},
         journal = {Organic Letters},
           pages = {1765 -- 1768},
            year = {2003},
             url = {http://d-scholarship-dev.library.pitt.edu/20452/},
        abstract = {(Matrix presented) Tandem radical cyclizations of suitably substituted N-aryl thiocarbamates, thioamides, and thioureas are induced by exposure to tris(trimethylsilyl)-silane (TTMSH) and UV light and provide furoquinolines, isofuroquinolines, cyclopentaquinolines, indoloquinolines, and related ring systems. The intermediacy of an {\ensuremath{\alpha}}-thioalkylamino radical, which is the synthetic equivalent of an imidoyl radical, is invoked.}
}